Canonical Allele Identifier: CA355514406

Gene: GHSR

Linked Data

• MyVariant Identifiers: chr3:g.172165744C>A (hg19) ; chr3:g.172447954C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172447954C>A , CM000665.2:g.172447954C>A	GRCh38
NC_000003.11:g.172165744C>A , CM000665.1:g.172165744C>A	GRCh37
NC_000003.10:g.173648438C>A	NCBI36
NG_021159.1:g.5503G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.460G>T MANE Select	ENSP00000241256.2:p.Val154Leu
ENST00000241256.2:c.460G>T	ENSP00000241256.2:p.Val154Leu
ENST00000427970.1:c.460G>T	ENSP00000395344.1:p.Val154Leu
NM_004122.2:c.460G>T	NP_004113.1:p.Val154Leu
NM_198407.2:c.460G>T MANE Select	NP_940799.1:p.Val154Leu